Test Price
2,800 AED✅ Home Collection Available
CC2D2A Gene COACH Syndrome Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين CC2D2A لمتلازمة كوتش بتقنية التسلسل الجيني المتقدم NGS في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO Accredited Processing.
Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain Home Collection and VIP Mobile Phlebotomy.
Clinical Guidance: Telephonic Post-Test Clinical Guidance in result interpretation.
Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
ضمان الدقة: حساسية تشخيصية تصل إلى 99.9% من خلال معالجة معتمدة من ISO. خدمة سحب دم منزلي فاخرة عبر فريق تمريض متنقل، مع استشارة سريرية هاتفية بعد الفحص.
Overview
This advanced genetic test utilises Next‑Generation Sequencing (NGS) to analyse the entire coding region of the CC2D2A gene, associated with COACH syndrome – a rare autosomal recessive disorder characterised by cerebellar vermis hypoplasia, oligophrenia, ataxia, coloboma, and hepatic fibrosis. It delivers precise variant detection to confirm clinical diagnosis, guide management, and inform family planning.
| Feature | Our Test: CC2D2A NGS Panel | Closest Alternative: Whole Exome Sequencing (WES) |
|---|---|---|
| Precision | Targeted >99.9% analytical sensitivity for CC2D2A variants | Broad coverage; may miss deep intronic or regulatory variants of single gene |
| Method | NGS with Sanger confirmation of all pathogenic findings | WES followed by bioinformatic filtering; often requires secondary Sanger |
| Speed | Results in 3–4 Weeks | 6–8 Weeks on average |
Physician Insight & Safety Protocol
“As a neurologist deeply invested in neurogenetics, I understand the profound anxiety families experience while awaiting molecular confirmation of COACH syndrome. This test provides definitive genetic evidence, but its results must always be integrated with clinical examination and neuroimaging findings. Never discontinue any prescribed medication or therapy without a thorough discussion with your treating physician.” — Dr. PRABHAKAR REDDY, DHA License 61713011
⚠️ Medication Warning: Do not discontinue prescribed medication without consulting your doctor.
Exclusion Criteria & ER Red Flags
- Exclusion: Inability to provide a peripheral blood sample (e.g., severe coagulopathy); lack of informed consent from a legal guardian for minors; active febrile illness that may interfere with sample integrity.
- Emergency Warning: If the patient experiences sudden neurological deterioration, new‑onset seizures, or signs of hepatic decompensation (jaundice, coagulopathy), seek immediate emergency care. This genetic test is not a substitute for acute clinical intervention.
Patient FAQ & Clinical Guidance
What does the CC2D2A gene test detect and why is it needed for COACH syndrome?
This NGS‑based analysis screens the entire CC2D2A gene for pathogenic variants that cause COACH syndrome, a condition marked by brain, eye, and liver abnormalities, thereby confirming the diagnosis and guiding lifelong multidisciplinary care.
يكشف تحليل جين CC2D2A عن الطفرات المسببة لمتلازمة كوتش، وهو اضطراب نادر يشمل تشوهات في الدماغ والعين والكبد، مما يؤكد التشخيص ويوجه الرعاية المتخصصة.
How is the sample collected and when will I receive my results?
A single blood draw or DNA sample is collected at your home by a certified mobile phlebotomist using cold‑chain logistics; the NGS testing is completed within 3–4 weeks, with telephonic counselling arranged upon report delivery.
يتم سحب عينة دم بسيطة في المنزل بواسطة ممرض متنقل، وتظهر نتائج التسلسل الجيني في غضون 3–4 أسابيع مع استشارة هاتفية.
Is this genetic covered by health insurance in the UAE?
Many UAE insurers reimburse medically necessary genetic testing for neurological disorders; our dedicated team verifies your policy benefits, handles pre‑authorisation, and offers direct billing to reduce out‑of‑pocket delays.
تغطي العديد من شركات التأمين في الإمارات الفحص الجيني الضروري طبياً، وسيقوم فريقنا بالتحقق من التغطية والتخليص المباشر.
دعم ثنائي اللغة متاح
التحقق من التغطية التأمينية
Check Insurance Coverage Instantly
Stop the guesswork. Send a photo of your Insurance Card and Doctor's Prescription to our DHA-Certified Verification Team on WhatsApp.
توقف عن التخمين. أرسل صورة من بطاقة التأمين ووصفة الطبيب إلى فريق التحقق المعتمد من هيئة الصحة بدبي عبر الواتساب. احصل على تحديث الحالة في دقائق.
Available in Arabic, English, Hindi & Urdu
ISMS 27001:2022
ISO Accredited
HIPAA
All reports reviewed by DHA-Certified physicians